反応式
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([Cl:8])[C:3]=1[C:9]1[C:20](=[O:21])[N:19]([CH3:22])[C:12]2[N:13]=[C:14](SC)[N:15]=[CH:16][C:11]=2[CH:10]=1.[CH2:23]([NH2:25])[CH3:24]>>[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([Cl:8])[C:3]=1[C:9]1[C:20](=[O:21])[N:19]([CH3:22])[C:12]2[N:13]=[C:14]([NH:25][CH2:23][CH3:24])[N:15]=[CH:16][C:11]=2[CH:10]=1参加物
3
実験手順
This compound was prepared by a procedure similar to that described in Example 40 starting with 6-(2,6-dichlorophenyl)-8-methyl-2-methylsulfanyl-8H-pyrido[2,3-d]pyrimidin-7-one of Example 37 and ethylamine gas; mp 180°-182° C.
後処理
- customThis compound was prepared by a procedure similar to
出典と根拠
- ORDレコード
- ord-32eed9b20fbe4a80a60b8ae09427c623
- 出典データセット
- uspto-grants-1998_03
- 特許番号
- US05733914
関連ノート
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